Variant report

Variant	rs12722711
Chromosome Location	chr10:6055245-6055246
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12243549	1.00[AMR][1000 genomes]
rs12243643	1.00[AMR][1000 genomes]
rs12258919	1.00[AMR][1000 genomes]
rs12722621	1.00[AMR][1000 genomes]
rs12722622	1.00[AMR][1000 genomes]
rs12722653	1.00[AMR][1000 genomes]
rs12722692	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12722697	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12722701	1.00[AMR][1000 genomes]
rs6602393	1.00[AMR][1000 genomes]
rs6602394	1.00[AMR][1000 genomes]
rs7896551	1.00[AMR][1000 genomes]
rs7917588	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34147	chr10:5726821-6105717	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	esv34061	chr10:5726821-6225187	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv1042286	chr10:5795129-6578445	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:6044000-6055800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr10:6048400-6055800	Weak transcription	K562	blood
3	chr10:6050000-6056000	Weak transcription	Primary T cells from cord blood	blood
4	chr10:6051200-6056000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr10:6051400-6056400	Weak transcription	NHEK	skin
6	chr10:6051800-6056000	Weak transcription	Adipose Nuclei	Adipose
7	chr10:6053000-6055800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr10:6053200-6055800	Strong transcription	Primary T helper cells PMA-I stimulated	--
9	chr10:6053200-6056000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr10:6054800-6055800	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr10:6054800-6055800	Weak transcription	Fetal Lung	lung
12	chr10:6055000-6056000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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